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rs863223433

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223433(A;A)
Make rs863223433(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43059226
GeneCBS
is asnp
is mentioned by
dbSNPrs863223433
ebirs863223433
HLIrs863223433
Exacrs863223433
Varsomers863223433
Maprs863223433
PheGenIrs863223433
hapmaprs863223433
1000 genomesrs863223433
hgdprs863223433
ensemblrs863223433
gopubmedrs863223433
geneviewrs863223433
scholarrs863223433
googlers863223433
pharmgkbrs863223433
gwascentralrs863223433
openSNPrs863223433
23andMers863223433
23andMe allrs863223433
SNP Nexus

SNPshotrs863223433
SNPdbers863223433
MSV3drs863223433
GWAS Ctlgrs863223433
Max Magnitude0
ClinVar
Risk rs863223433(A;A)
Alt rs863223433(A;A)
Reference rs863223433(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.44479336C>T
CLNSRC
CLNACC RCV000196138.1,